Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 6:52419426 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.52419426A>G

About this variant

This variant overlaps 4 transcripts and has 2504 individual genotypes.

Variation displays